Synthesis and evaluation of biodegradable segmented multiblock poly(ether ester) copolymers for biomaterial applications

Based on 1,4‐succinic acid, 1,4‐butanediol, poly(ethylene glycol)s and dimethyl terephthalate, biodegradable segmented multiblock copolymers of poly[(butylene terephthalate)‐co‐poly(butylene succinate)‐block‐poly(ethylene glycol)] (PTSG) were synthesized with different poly(butylene succinate) (PBS)...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Polymer international 2004-12, Vol.53 (12), p.2145-2154
Hauptverfasser: Wang, Lian-cai, Chen, Jin-wu, Liu, Hou-li, Chen, Zhu-qiong, Zhang, Yong, Wang, Chang-yong, Feng, Zeng-guo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2154
container_issue 12
container_start_page 2145
container_title Polymer international
container_volume 53
creator Wang, Lian-cai
Chen, Jin-wu
Liu, Hou-li
Chen, Zhu-qiong
Zhang, Yong
Wang, Chang-yong
Feng, Zeng-guo
description Based on 1,4‐succinic acid, 1,4‐butanediol, poly(ethylene glycol)s and dimethyl terephthalate, biodegradable segmented multiblock copolymers of poly[(butylene terephthalate)‐co‐poly(butylene succinate)‐block‐poly(ethylene glycol)] (PTSG) were synthesized with different poly(butylene succinate) (PBS) molar fractions and varying the poly(ethylene glycol) (PEG) segment length, and were evaluated as biomedical materials. The copolymer extracts showed no in vitro cytotoxicity. However, sterilization of the copolymers by gamma irradiation had some limited effect on the cytotoxicity and mechanical properties. A copolymer consisting of PEG‐1000 and 20 mol% PBS, assigned as 1000PBS20 after SO2 gas plasma treatment, sustained the adhesion and growth of dog vascular smooth muscle cells. The in vivo biocompatibility of this sample was also measured subcutaneously in rats for 4 weeks. The assessments indicated that these poly(ether ester) copolymers are good candidates for anti‐adhesion barrier and drug controlled‐release applications. Copyright © 2004 Society of Chemical Industry
doi_str_mv 10.1002/pi.1645
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_28778314</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>28413984</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3915-7ae8ee1dfb7ed883a2c3db1db258defbdf4289032e50372c7e39da87137881383</originalsourceid><addsrcrecordid>eNqN0d9r1TAUwPEiCl6n-C_kRZ1IZ360TfLohpsbFx1M0bdwmpzOuLSpSe_c_e9tvZf5JPgUOPnwJeQUxXNGjxil_O3oj1hT1Q-KFaNalpTx5mGxorrWpWJUPC6e5PyDUqq01qvi7mo7TN8x-0xgcARvIWxg8nEgsSOtjw6vEzhoA5KM1z0OEzrSb8Lk2xDtDRlj2B7iXEgE84TpNbFxmfWYMuliWho9zBceAoFxDN7-yeenxaMOQsZn-_Og-HL6_vPJh3L96ez85N26tEKzupSACpG5rpXolBLArXAtcy2vlcOudV3FlaaCY02F5Fai0A6UZEIqxYQSB8XLXXdM8edmfqPpfbYYAgwYN9lwJaUSrPoPWDGh1QJf7aBNMeeEnRmT7yFtDaNmWYEZvVlWMMsX-yRkC6FLMFif__KGN1xXenZvdu6XD7j9V85cnu-r5U77-cPv7jWkG9NIIWvz9eOZubqsj6v1twsjxW9IfKWl</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>28413984</pqid></control><display><type>article</type><title>Synthesis and evaluation of biodegradable segmented multiblock poly(ether ester) copolymers for biomaterial applications</title><source>Access via Wiley Online Library</source><creator>Wang, Lian-cai ; Chen, Jin-wu ; Liu, Hou-li ; Chen, Zhu-qiong ; Zhang, Yong ; Wang, Chang-yong ; Feng, Zeng-guo</creator><creatorcontrib>Wang, Lian-cai ; Chen, Jin-wu ; Liu, Hou-li ; Chen, Zhu-qiong ; Zhang, Yong ; Wang, Chang-yong ; Feng, Zeng-guo</creatorcontrib><description>Based on 1,4‐succinic acid, 1,4‐butanediol, poly(ethylene glycol)s and dimethyl terephthalate, biodegradable segmented multiblock copolymers of poly[(butylene terephthalate)‐co‐poly(butylene succinate)‐block‐poly(ethylene glycol)] (PTSG) were synthesized with different poly(butylene succinate) (PBS) molar fractions and varying the poly(ethylene glycol) (PEG) segment length, and were evaluated as biomedical materials. The copolymer extracts showed no in vitro cytotoxicity. However, sterilization of the copolymers by gamma irradiation had some limited effect on the cytotoxicity and mechanical properties. A copolymer consisting of PEG‐1000 and 20 mol% PBS, assigned as 1000PBS20 after SO2 gas plasma treatment, sustained the adhesion and growth of dog vascular smooth muscle cells. The in vivo biocompatibility of this sample was also measured subcutaneously in rats for 4 weeks. The assessments indicated that these poly(ether ester) copolymers are good candidates for anti‐adhesion barrier and drug controlled‐release applications. Copyright © 2004 Society of Chemical Industry</description><identifier>ISSN: 0959-8103</identifier><identifier>EISSN: 1097-0126</identifier><identifier>DOI: 10.1002/pi.1645</identifier><language>eng</language><publisher>Chichester, UK: John Wiley &amp; Sons, Ltd</publisher><subject>Applied sciences ; biocompatibility ; Biological and medical sciences ; cell adhesion ; cytotoxicity ; degradation ; Exact sciences and technology ; Medical sciences ; Organic polymers ; Physicochemistry of polymers ; poly(ether ester) ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; Technology. Biomaterials. Equipments. Material. Instrumentation</subject><ispartof>Polymer international, 2004-12, Vol.53 (12), p.2145-2154</ispartof><rights>2004 Society of Chemical Industry</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3915-7ae8ee1dfb7ed883a2c3db1db258defbdf4289032e50372c7e39da87137881383</citedby><cites>FETCH-LOGICAL-c3915-7ae8ee1dfb7ed883a2c3db1db258defbdf4289032e50372c7e39da87137881383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpi.1645$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpi.1645$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16262949$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Lian-cai</creatorcontrib><creatorcontrib>Chen, Jin-wu</creatorcontrib><creatorcontrib>Liu, Hou-li</creatorcontrib><creatorcontrib>Chen, Zhu-qiong</creatorcontrib><creatorcontrib>Zhang, Yong</creatorcontrib><creatorcontrib>Wang, Chang-yong</creatorcontrib><creatorcontrib>Feng, Zeng-guo</creatorcontrib><title>Synthesis and evaluation of biodegradable segmented multiblock poly(ether ester) copolymers for biomaterial applications</title><title>Polymer international</title><addtitle>Polym. Int</addtitle><description>Based on 1,4‐succinic acid, 1,4‐butanediol, poly(ethylene glycol)s and dimethyl terephthalate, biodegradable segmented multiblock copolymers of poly[(butylene terephthalate)‐co‐poly(butylene succinate)‐block‐poly(ethylene glycol)] (PTSG) were synthesized with different poly(butylene succinate) (PBS) molar fractions and varying the poly(ethylene glycol) (PEG) segment length, and were evaluated as biomedical materials. The copolymer extracts showed no in vitro cytotoxicity. However, sterilization of the copolymers by gamma irradiation had some limited effect on the cytotoxicity and mechanical properties. A copolymer consisting of PEG‐1000 and 20 mol% PBS, assigned as 1000PBS20 after SO2 gas plasma treatment, sustained the adhesion and growth of dog vascular smooth muscle cells. The in vivo biocompatibility of this sample was also measured subcutaneously in rats for 4 weeks. The assessments indicated that these poly(ether ester) copolymers are good candidates for anti‐adhesion barrier and drug controlled‐release applications. Copyright © 2004 Society of Chemical Industry</description><subject>Applied sciences</subject><subject>biocompatibility</subject><subject>Biological and medical sciences</subject><subject>cell adhesion</subject><subject>cytotoxicity</subject><subject>degradation</subject><subject>Exact sciences and technology</subject><subject>Medical sciences</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>poly(ether ester)</subject><subject>Polymers with particular properties</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>Technology. Biomaterials. Equipments. Material. Instrumentation</subject><issn>0959-8103</issn><issn>1097-0126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqN0d9r1TAUwPEiCl6n-C_kRZ1IZ360TfLohpsbFx1M0bdwmpzOuLSpSe_c_e9tvZf5JPgUOPnwJeQUxXNGjxil_O3oj1hT1Q-KFaNalpTx5mGxorrWpWJUPC6e5PyDUqq01qvi7mo7TN8x-0xgcARvIWxg8nEgsSOtjw6vEzhoA5KM1z0OEzrSb8Lk2xDtDRlj2B7iXEgE84TpNbFxmfWYMuliWho9zBceAoFxDN7-yeenxaMOQsZn-_Og-HL6_vPJh3L96ez85N26tEKzupSACpG5rpXolBLArXAtcy2vlcOudV3FlaaCY02F5Fai0A6UZEIqxYQSB8XLXXdM8edmfqPpfbYYAgwYN9lwJaUSrPoPWDGh1QJf7aBNMeeEnRmT7yFtDaNmWYEZvVlWMMsX-yRkC6FLMFif__KGN1xXenZvdu6XD7j9V85cnu-r5U77-cPv7jWkG9NIIWvz9eOZubqsj6v1twsjxW9IfKWl</recordid><startdate>200412</startdate><enddate>200412</enddate><creator>Wang, Lian-cai</creator><creator>Chen, Jin-wu</creator><creator>Liu, Hou-li</creator><creator>Chen, Zhu-qiong</creator><creator>Zhang, Yong</creator><creator>Wang, Chang-yong</creator><creator>Feng, Zeng-guo</creator><general>John Wiley &amp; Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope></search><sort><creationdate>200412</creationdate><title>Synthesis and evaluation of biodegradable segmented multiblock poly(ether ester) copolymers for biomaterial applications</title><author>Wang, Lian-cai ; Chen, Jin-wu ; Liu, Hou-li ; Chen, Zhu-qiong ; Zhang, Yong ; Wang, Chang-yong ; Feng, Zeng-guo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3915-7ae8ee1dfb7ed883a2c3db1db258defbdf4289032e50372c7e39da87137881383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Applied sciences</topic><topic>biocompatibility</topic><topic>Biological and medical sciences</topic><topic>cell adhesion</topic><topic>cytotoxicity</topic><topic>degradation</topic><topic>Exact sciences and technology</topic><topic>Medical sciences</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>poly(ether ester)</topic><topic>Polymers with particular properties</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>Technology. Biomaterials. Equipments. Material. Instrumentation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Lian-cai</creatorcontrib><creatorcontrib>Chen, Jin-wu</creatorcontrib><creatorcontrib>Liu, Hou-li</creatorcontrib><creatorcontrib>Chen, Zhu-qiong</creatorcontrib><creatorcontrib>Zhang, Yong</creatorcontrib><creatorcontrib>Wang, Chang-yong</creatorcontrib><creatorcontrib>Feng, Zeng-guo</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymer international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Lian-cai</au><au>Chen, Jin-wu</au><au>Liu, Hou-li</au><au>Chen, Zhu-qiong</au><au>Zhang, Yong</au><au>Wang, Chang-yong</au><au>Feng, Zeng-guo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and evaluation of biodegradable segmented multiblock poly(ether ester) copolymers for biomaterial applications</atitle><jtitle>Polymer international</jtitle><addtitle>Polym. Int</addtitle><date>2004-12</date><risdate>2004</risdate><volume>53</volume><issue>12</issue><spage>2145</spage><epage>2154</epage><pages>2145-2154</pages><issn>0959-8103</issn><eissn>1097-0126</eissn><abstract>Based on 1,4‐succinic acid, 1,4‐butanediol, poly(ethylene glycol)s and dimethyl terephthalate, biodegradable segmented multiblock copolymers of poly[(butylene terephthalate)‐co‐poly(butylene succinate)‐block‐poly(ethylene glycol)] (PTSG) were synthesized with different poly(butylene succinate) (PBS) molar fractions and varying the poly(ethylene glycol) (PEG) segment length, and were evaluated as biomedical materials. The copolymer extracts showed no in vitro cytotoxicity. However, sterilization of the copolymers by gamma irradiation had some limited effect on the cytotoxicity and mechanical properties. A copolymer consisting of PEG‐1000 and 20 mol% PBS, assigned as 1000PBS20 after SO2 gas plasma treatment, sustained the adhesion and growth of dog vascular smooth muscle cells. The in vivo biocompatibility of this sample was also measured subcutaneously in rats for 4 weeks. The assessments indicated that these poly(ether ester) copolymers are good candidates for anti‐adhesion barrier and drug controlled‐release applications. Copyright © 2004 Society of Chemical Industry</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><doi>10.1002/pi.1645</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0959-8103
ispartof Polymer international, 2004-12, Vol.53 (12), p.2145-2154
issn 0959-8103
1097-0126
language eng
recordid cdi_proquest_miscellaneous_28778314
source Access via Wiley Online Library
subjects Applied sciences
biocompatibility
Biological and medical sciences
cell adhesion
cytotoxicity
degradation
Exact sciences and technology
Medical sciences
Organic polymers
Physicochemistry of polymers
poly(ether ester)
Polymers with particular properties
Preparation, kinetics, thermodynamics, mechanism and catalysts
Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)
Technology. Biomaterials. Equipments. Material. Instrumentation
title Synthesis and evaluation of biodegradable segmented multiblock poly(ether ester) copolymers for biomaterial applications
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T08%3A57%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20evaluation%20of%20biodegradable%20segmented%20multiblock%20poly(ether%20ester)%20copolymers%20for%20biomaterial%20applications&rft.jtitle=Polymer%20international&rft.au=Wang,%20Lian-cai&rft.date=2004-12&rft.volume=53&rft.issue=12&rft.spage=2145&rft.epage=2154&rft.pages=2145-2154&rft.issn=0959-8103&rft.eissn=1097-0126&rft_id=info:doi/10.1002/pi.1645&rft_dat=%3Cproquest_cross%3E28413984%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=28413984&rft_id=info:pmid/&rfr_iscdi=true